Canonical Allele Identifier: CA2138218438

Gene: GCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54844693G= , CM000676.2:g.54844693G=	GRCh38
NC_000014.8:g.55311411G= , CM000676.1:g.55311411G=	GRCh37
NC_000014.7:g.54381161G=	NCBI36
NG_008647.1:g.63132C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000491895.7:c.627-550C= MANE Select	ENSP00000419045.2:n.627-550C=
ENST00000254299.8:n.775-550C=
ENST00000395514.5:c.627-550C=	ENSP00000378890.1:n.627-550C=
ENST00000395521.6:n.293-1639C=
ENST00000491895.6:c.627-550C=	ENSP00000419045.2:n.627-550C=
ENST00000536224.2:c.626+1075C=	ENSP00000445246.2:n.626+1075C=
ENST00000543643.6:c.627-824C=	ENSP00000444011.2:n.627-824C=
ENST00000622544.4:c.627-550C=	ENSP00000477796.1:n.627-550C=
NM_000161.2:c.627-550C=	NP_000152.1:n.627-550C=
NM_001024024.1:c.627-550C=	NP_001019195.1:n.627-550C=
NM_001024070.1:c.627-824C=	NP_001019241.1:n.627-824C=
NM_001024071.1:c.626+1075C=	NP_001019242.1:n.626+1075C=
XM_005267530.1:c.627-824C=	XP_005267587.1:n.627-824C=
XM_017021218.1:c.333-550C=	XP_016876707.1:n.333-550C=
NM_000161.3:c.627-550C= MANE Select	NP_000152.1:n.627-550C=
NM_001024070.2:c.627-824C=	NP_001019241.1:n.627-824C=
NM_001024071.2:c.626+1075C=	NP_001019242.1:n.626+1075C=
NM_001024024.2:c.627-550C=	NP_001019195.1:n.627-550C=